A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3589169



Internal ID6629458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234392482..234485360hg38UCSC Ensembl
chr1:234528228..234621106hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg3892879
hg1992879
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10330260
SamplesHG02449
Known GenesTARBP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3589169
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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